Inovo, Inc, Economizer Conserving Regulator

FDA 510(k) K031983 · Inovo, Inc.

Substantially Equivalent

510(k) numberK031983

Submission

Device name
Inovo, Inc, Economizer Conserving Regulator
Applicant
Inovo, Inc.
Great Neck, NY, US
Received
June 26, 2003
Decision date
September 15, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NFB – Conserver, Oxygen
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5905
Specialty
Anesthesiology

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K131023Theraflow Single Lumen and Theraflow Dual LumenNFB · Traditional Medical Products, LLC10/11/2013SE
K113111Chad Therapeutic Evolution Electronic Oxygen Conserver with MotionNFB · Special Inovo, Inc.12/08/2011SE
K103392Chad Therapeutic Evolution Electronic Oxygen ConserverNFB · Special Inovo, Inc.12/17/2010SE
K090421Model 350G Gas ConserverNFB · Traditional Inspired Technologies, Inc.05/29/2009SE
K070740Chad Therapeutics Bonsai Model 800NFB · Special Chad Therapeutics, Inc.05/07/2007SE

More from Chad Therapeutics, Inc.

510(k)DeviceDecision
K141967Purefill Oxygen CompressorCAW · Traditional 11/07/2014SE
K113111Chad Therapeutic Evolution Electronic Oxygen Conserver with MotionNFB · Special 12/08/2011SE
K103392Chad Therapeutic Evolution Electronic Oxygen ConserverNFB · Special 12/17/2010SE
K060751Inovo, Inc. Accupulse Single Lumen Conserving RegulatorNFB · Traditional 07/18/2006SE
K051540Inovo, Inc. Independence Oxygen Conserving RegulatorNFB · Traditional 09/21/2005SE

Questions and answers

When was Inovo, Inc, Economizer Conserving Regulator cleared by the FDA?

Inovo, Inc, Economizer Conserving Regulator (K031983) received a 510(k) decision of Substantially Equivalent on September 15, 2003, 81 days after the submission was received.

What is the product code of K031983?

The FDA product code is NFB – Conserver, Oxygen, a Class II (moderate risk) device regulated under 21 CFR 868.5905.